CAS 81731-43-3
:Aminoethylisopropylether; 98%
Description:
Aminoethylisopropylether, with the CAS number 81731-43-3, is an organic compound characterized by the presence of both amino and ether functional groups. This substance typically appears as a colorless to pale yellow liquid and is known for its moderate viscosity. It is soluble in water and various organic solvents, making it versatile for different applications. The compound exhibits properties such as being hygroscopic, which means it can absorb moisture from the air. Its amino group contributes to its reactivity, allowing it to participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Aminoethylisopropylether is often utilized in the synthesis of pharmaceuticals, agrochemicals, and as a surfactant or emulsifier in industrial applications. Safety data indicates that it should be handled with care, as it may cause irritation to the skin, eyes, and respiratory system upon exposure. Proper safety measures, including the use of personal protective equipment, are recommended when working with this chemical.
Formula:C5H13NO
InChI:InChI=1/C5H13NO/c1-5(2)7-4-3-6/h5H,3-4,6H2,1-2H3
SMILES:CC(C)OCCN
Synonyms:- 2-Aminoethyl isopropyl ether
- 2-(Propan-2-Yloxy)Ethanamine
- 2-Isopropoxy-Ethylamine
- ASINEX-REAG BAS 07679786
- 2-Aminoethyl Isopropyl Ether >
- 2-Isopropoxyethan-1-amine
- aminoethylisopropylether
- 2-(1-methylethoxy)Ethanamine
- 2-isopropoxyethanaMine
- 2-ISOPROPOXYETHYLAMINE
- Ethanamine, 2-(1-methylethoxy)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
2-Aminoethyl Isopropyl Ether
CAS:Formula:C5H13NOPurity:>98.0%(GC)(T)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:103.172-Aminoethyl isopropyl ether
CAS:Formula:C5H13NOPurity:95%Color and Shape:LiquidMolecular weight:103.1652-Aminoethyl isopropylether
CAS:<p>2-Aminoethyl isopropylether (2-AP) has been shown to have inhibitory effects on the growth of Staphylococcus aureus, Bacillus subtilis and Escherichia coli. It also showed in vitro antifungal activity against Trichophyton mentagrophytes and Candida albicans. 2-AP inhibits the synthesis of unsaturated fatty acids by inhibiting the enzyme enoyl coenzyme A reductase, which is involved in the degradation of fatty acids. 2-AP is metabolized by two pathways: one is through hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid; the other pathway involves cyclobutanol formation. The cytotoxic effect of 2-AP has been shown to be due to inhibition of protein synthesis and cell division</p>Formula:C5H13NOPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:103.16 g/mol




